Desiree Nock-Chester

CRS:

JHU

Role:

Research Staff

Position:

Research Assistant

Email:

dnock1@jhmi.edu

Desiree Nock-Chester responsible for QA/QC. Her duties include QA/QC of charts and crf binders, visit prep, creating laboratory requisitions, resolving queries and delinquencies, transcription, data entry, and maintaining error reports.

She has been a part of the data staff of the ACTG  at Johns Hopkins University for more than 10 years. She began as the transcriptionist for the unit and held that position for nearly 3 years. Prior to joining the clinical trials unit, Ms. Nock-Chester worked in the Wilmer at  Johns Hopkins for 9 years as a Sr. Patient Services Coordinator. Her  duties included registering patients for appointments, surgeries, post-op visits, verifying insurance information, obtaining referrals, and balancing out the daily intake of co-payments.

Categories

Leadership Committees
CRS
Roles

Clinical Trials

A5342: Evaluating the Safety, Tolerability, and Effect of a...

The purpose of this study is to evaluate the safety, tolerability, and effect of an experimental human monoclonal antibody...

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P1077FF: Formula Feeding Version of the PROMISE Study...

1077FF is a randomized strategy trial, which is part of the PROMISE studies (1077BF, 1077FF, P1084s, and 1077HS). The Promoting...

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A5282: A Randomized, Phase II Trial to Compare an HPV...

The investigators are looking for a better way to prevent cervical cancer. This study is comparing two different methods to...

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A5128: Consent for Use of Stored Patient Specimens for...

The purpose of this study is to obtain informed consent to use stored human biological materials (HBM) (e.g., blood and other...

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A5300/P2003: PHOENIx Feasibility Study

Study of MDR TB Cases and Their Household Contacts: Operational Feasibility to Inform PHOENIx Trial Design

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